화학공학소재연구정보센터
Journal of Vacuum Science & Technology A, Vol.21, No.5, 1649-1654, 2003
Optimization of secondary ion mass spectrometry detection limit for N in SiC
Controlled changes in the Cs+ primary ion beam density and analytical expressions describing the sources (bulk concentration, memory effect, and adsorption of N from the residual vacuum) of secondary ion mass spectrometry analyte secondary ion intensities were used to determine the contributions to the N secondary ion intensity obtained during the analysis of trace levels of N in bulk SiC. This methodology allows the determination of N concentrations that can be substantially less than the apparent N secondary ion background intensity. It was shown that for the Cameca IMS-6F instrumental conditions used, memory effect is the main contributor to the N background signal. Taking into consideration the Cs+ beam diameter, the raster size, the diameter of the ion-extracted area, and the impurity secondary ion intensity, an optimized combination of primary ion beam current and raster size was determined that resulted in the best detection limit for N in bulk SiC. This detection limit for N in bulk SiC (similar to6 X 10(14) atoms/cm(3)) was obtained for a primary ion current of 100 nA, a faster size of 45 mumX45 mum, and a secondary ion extraction area diameter of 30 mum. (C) 2003 American Vacuum Society.